ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA159592
Gene: FANCG
HGNC
NCBI
Linked Data
ClinVar Variation Id:
134357
ClinVar RCV Id:
RCV000121031
RCV001166629
RCV000860702
RCV003430676
RCV003925190
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_004620.1:p.Gln26Arg
CA159590
NM_004629.2:c.77A>G